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rs770285398

From SNPedia

Orientationplus
Geno Mag Summary
(TTGT;TTGT) 0 common in clinvar
Make rs770285398(-;-)
Make rs770285398(-;TTGT)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position64616217
GeneCYP7B1
is asnp
is mentioned by
dbSNPrs770285398
ebirs770285398
HLIrs770285398
Exacrs770285398
Varsomers770285398
Maprs770285398
PheGenIrs770285398
hapmaprs770285398
1000 genomesrs770285398
hgdprs770285398
ensemblrs770285398
gopubmedrs770285398
geneviewrs770285398
scholarrs770285398
googlers770285398
pharmgkbrs770285398
gwascentralrs770285398
openSNPrs770285398
23andMers770285398
23andMe allrs770285398
SNP Nexus

SNPshotrs770285398
SNPdbers770285398
MSV3drs770285398
GWAS Ctlgrs770285398
Max Magnitude0
ClinVar
Risk rs770285398(;)
Alt rs770285398(;)
Reference rs770285398(TTGT;TTGT)
Significance Pathogenic
Disease Spastic paraplegia
Variation info
Gene CYP7B1
CLNDBN Spastic paraplegia
Reversed 0
HGVS NC_000008.10:g.65528774_65528777delTTGT
CLNSRC
CLNACC RCV000227207.1,